A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7682



Internal ID15206030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12066826..12101962hg38UCSC Ensembl
Outerchr11:12088373..12123509hg19UCSC Ensembl
Outerchr11:12044949..12080085hg18UCSC Ensembl
Outerchr11:12044949..12080085hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384610
hg194610
hg184610
hg174610
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3927
SamplesNA12878
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7682
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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